A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499745



Internal ID22557681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:160017098..160077582hg38UCSC Ensembl
chr4:160938250..160998734hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3860485
hg1960485
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837780
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499745
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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